Run ID: ERR2516071
Sample name:
Date: 31-03-2023 21:16:20
Number of reads: 409189
Percentage reads mapped: 99.7
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288769 | c.472delG | frameshift_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6808 | c.-494C>A | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491515 | p.Asn245His | missense_variant | 0.15 |
mshA | 576154 | c.807C>T | synonymous_variant | 0.12 |
ccsA | 620732 | p.Ala281Val | missense_variant | 0.17 |
rpoB | 762189 | p.Ile795Val | missense_variant | 0.13 |
rpoC | 764922 | p.Glu518Gly | missense_variant | 0.11 |
rpoC | 765452 | p.Ala695Thr | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776086 | p.Val799Ile | missense_variant | 0.12 |
mmpL5 | 776175 | p.Ser769Phe | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406386 | p.Ala319Ser | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476096 | n.2439T>G | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1833400 | c.-141delC | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101712 | p.Gln444Leu | missense_variant | 0.11 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169149 | c.1464G>C | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.29 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.25 |
PPE35 | 2170662 | c.-50G>A | upstream_gene_variant | 0.18 |
Rv1979c | 2222470 | p.Phe232Ser | missense_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714698 | p.Arg212His | missense_variant | 0.12 |
folC | 2746547 | p.Asp351Gly | missense_variant | 0.13 |
pepQ | 2859310 | p.Ala370Gly | missense_variant | 0.29 |
pepQ | 2860295 | p.Ala42Pro | missense_variant | 0.12 |
ribD | 2987560 | p.Ala241Asp | missense_variant | 0.14 |
Rv2752c | 3064814 | p.Ile460Leu | missense_variant | 0.17 |
Rv3236c | 3612133 | c.984C>T | synonymous_variant | 0.2 |
Rv3236c | 3612910 | p.Leu69Phe | missense_variant | 0.25 |
fbiB | 3641016 | c.-519C>T | upstream_gene_variant | 0.1 |
alr | 3840828 | c.592dupG | frameshift_variant | 0.11 |
alr | 3841515 | c.-95C>T | upstream_gene_variant | 0.15 |
alr | 3841535 | c.-115G>A | upstream_gene_variant | 0.13 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.1 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
clpC1 | 4040241 | p.Thr155Phe | missense_variant | 0.11 |
clpC1 | 4040249 | p.Glu152Gly | missense_variant | 0.12 |
embC | 4239993 | c.133_135delATC | conservative_inframe_deletion | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244332 | p.Val367Glu | missense_variant | 0.22 |
embA | 4245244 | p.Ala671Asp | missense_variant | 0.12 |
embA | 4246255 | p.Leu1008Pro | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |